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Iron Deficiency Anemia clinical trials

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NCT ID: NCT00298441 Completed - Hemodialysis Clinical Trials

Efficacy of Intravenous Iron Administration in Hemodialysis Patients

Start date: June 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the frequency of intravenous iron administration has an effect on anemia correction and oxidative stress formation in hemodialysis patients.

NCT ID: NCT00298051 Completed - Clinical trials for Iron-deficiency Anemia

Umbilical Cord Clamping and Infant Iron Status

Start date: October 2003
Phase: N/A
Study type: Interventional

The aim of the study was to determine whether delayed umbilical cord clamping, as compared to early umbilical cord clamping, improves infant iron status at 6 months of age.

NCT ID: NCT00284700 Completed - Clinical trials for Helicobacter Pylori Infection

Is Helicobacter Pylori Infection a Cause or Treatment Failure of Iron Deficiency Anemia in Children in Bangladesh?

Start date: December 1997
Phase: N/A
Study type: Interventional

Helicobacter pylori is recognized as a major gastrointestinal pathogen in developing countries. This microorganism infects up to 60% of children less than five years in those countries and is strongly associated with chronic gastritis and peptic ulcer disease in children and adults. The progression of gastritis to atrophy often leads to decreased gastric acid output, which is a well-known risk factor for anemia. Gastric acid is essential for increasing the bioavailability and absorption of non-heme dietary iron, the most important source of iron in developing countries. Numerous reports suggest that iron malabsorption secondary to low gastric acid output is a problem in developing world countries. It has been further observed that iron deficiency anemia is resistant to iron therapy particularly in these countries. In a recently completed study we observed an association of anaemia with H. pylori infection. We hypothesize that the poor bioavailability of iron in these countries could be related to H. pylori -induced low gastric acid output and we propose to investigate the role of H. pylori infection as a cause of anemia and treatment failure of iron supplementation in Bangladesh. A prospective, randomized, double-blind, placebo-controlled field trial is proposed among four groups ( 65 each) of H. Pylori infected children of 2-5 years of age with iron deficiency anemia. The children will be assigned to one of the four therapies: antibiotics alone (for H. Pylori eradication), antibiotic plus iron therapy, iron therapy alone, or placebo. Hemoglobin concentration, serum ferritin concentration, and transferrin receptor will be measured before and at 1 and 3 month after the intervention. We also propose a complementary study in an additional 20 children with H. Pylori infection and iron deficiency anemia to assess iron absorption with application of double stable isotopes. The change in hematological parameters will also be compared among the groups before and after the therapy. The results of this study are expected to have implications in the prevention and treatment of iron deficiency anemia in developing countries.

NCT ID: NCT00276198 Completed - Clinical trials for Iron Deficiency Anemia

Efficacy Trial to Examine Efficacy of Multimicronutrient Home Supplementation in Infants

Start date: July 2005
Phase: Phase 3
Study type: Interventional

The objective of the program is to examine the efficacy of 6 month home micronutrient supplementation in Bedouin and Jewish children on improvements in nutritional status including measures of iron, ferritin, zinc and folic acid, and measures of growth and health parameters i.e.reported and recorded morbidity.

NCT ID: NCT00223977 Completed - Clinical trials for Iron Deficiency Anemia

2 Doses of Ferrlecit Versus Oral Iron to Treat Iron-deficiency Anemia in Peritoneal Dialysis Patients.

Start date: December 2003
Phase: Phase 2/Phase 3
Study type: Interventional

This is a phase 3 clinical investigation. Patients who meet the eligibility criteria and provide signed informed consent will be randomized to receive one of two levels of Ferrlecit or oral iron in a 1:1:1 ratio.

NCT ID: NCT00202488 Completed - Clinical trials for Helicobacter Pylori Infection

The Effect of H. Pylori Infection on Iron Metabolism

Start date: November 2002
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if Helicobacter pylori (H. pylori) gastritis results in abnormal iron metabolism in patients with iron deficiency anemia (IDA), and to determine if this is due to strain variations in the H. pylori organism.

NCT ID: NCT00198848 Completed - Clinical trials for Iron Deficiency Anemia

Iron Supplementation Among Adolescent Girls in India

Start date: September 2005
Phase: N/A
Study type: Interventional

This study will implement and evaluate a community-based intervention to distribute and promote consumption of weekly iron-folic acid supplements and to provide nutrition education to reduce the prevalence of iron deficiency anemia among adolescent girls in West Bengal, India.